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Triggerable Multivalent Glyconanoparticles for Probing Carbohydrate–Carbohydrate Interactions
[Image: see text] Carbohydrate–carbohydrate interactions are proposed to be biologically significant but have lower affinities than the well-studied carbohydrate–protein interactions. Here we introduce multivalent glyconanostructures where the surface expression of lactose can be triggered by an ext...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5894439/ https://www.ncbi.nlm.nih.gov/pubmed/29657901 http://dx.doi.org/10.1021/acsmacrolett.7b00891 |
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author | Won, Sangho Hindmarsh, Steven Gibson, Matthew I. |
author_facet | Won, Sangho Hindmarsh, Steven Gibson, Matthew I. |
author_sort | Won, Sangho |
collection | PubMed |
description | [Image: see text] Carbohydrate–carbohydrate interactions are proposed to be biologically significant but have lower affinities than the well-studied carbohydrate–protein interactions. Here we introduce multivalent glyconanostructures where the surface expression of lactose can be triggered by an external stimulus, and a gold nanoparticle core enables colorimetric signal outputs to probe binding. Macromolecular engineering of a responsive polymer “gate” enables the lactose moieties to be presented only when an external stimulus is present, mimicking how nature uses enzymes to dynamically regulate glycan expression. Two different carbohydrate–carbohydrate interactions are investigated using this tool. |
format | Online Article Text |
id | pubmed-5894439 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-58944392018-04-12 Triggerable Multivalent Glyconanoparticles for Probing Carbohydrate–Carbohydrate Interactions Won, Sangho Hindmarsh, Steven Gibson, Matthew I. ACS Macro Lett [Image: see text] Carbohydrate–carbohydrate interactions are proposed to be biologically significant but have lower affinities than the well-studied carbohydrate–protein interactions. Here we introduce multivalent glyconanostructures where the surface expression of lactose can be triggered by an external stimulus, and a gold nanoparticle core enables colorimetric signal outputs to probe binding. Macromolecular engineering of a responsive polymer “gate” enables the lactose moieties to be presented only when an external stimulus is present, mimicking how nature uses enzymes to dynamically regulate glycan expression. Two different carbohydrate–carbohydrate interactions are investigated using this tool. American Chemical Society 2018-01-18 2018-02-20 /pmc/articles/PMC5894439/ /pubmed/29657901 http://dx.doi.org/10.1021/acsmacrolett.7b00891 Text en Copyright © 2018 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Won, Sangho Hindmarsh, Steven Gibson, Matthew I. Triggerable Multivalent Glyconanoparticles for Probing Carbohydrate–Carbohydrate Interactions |
title | Triggerable Multivalent Glyconanoparticles for Probing
Carbohydrate–Carbohydrate Interactions |
title_full | Triggerable Multivalent Glyconanoparticles for Probing
Carbohydrate–Carbohydrate Interactions |
title_fullStr | Triggerable Multivalent Glyconanoparticles for Probing
Carbohydrate–Carbohydrate Interactions |
title_full_unstemmed | Triggerable Multivalent Glyconanoparticles for Probing
Carbohydrate–Carbohydrate Interactions |
title_short | Triggerable Multivalent Glyconanoparticles for Probing
Carbohydrate–Carbohydrate Interactions |
title_sort | triggerable multivalent glyconanoparticles for probing
carbohydrate–carbohydrate interactions |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5894439/ https://www.ncbi.nlm.nih.gov/pubmed/29657901 http://dx.doi.org/10.1021/acsmacrolett.7b00891 |
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